A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv953563



Internal ID17302437
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr18:77097945..77109944hg38UCSC Ensembl
Outerchr18:74809901..74821900hg19UCSC Ensembl
Cytoband18q23
Allele length
AssemblyAllele length
hg3812000
hg1912000
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2998898
SamplesBILGI_BIOE
Known GenesMBP
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nsv953563
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer